
200 open roles · Clinical
Clinical Research Associate II
- Added to ZestAmigo
- Last seen on employer site
Where you can work
Remote
Eligibility not captured
Locations named in the listing
- Saint-Maur-des-Fossés, Île-de-France, France
View location wording from the posting
Saint-Maur-des-Fossés, IDF, France
Role overview
Extracted from the posting. Read the employer’s full description below.
What they are looking for
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in France
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in oncology, hemophilia, infectious diseases, GI
- Full working proficiency in English
Show all 9 itemsShow fewer items
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Employer description
Company Description
PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
You will:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in France
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in oncology, hemophilia, infectious diseases, GI
- Full working proficiency in English
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Additional Information
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
We offer:
- Big professional advancement opportunity within Clinical Operations with specific mentorship and training program
- Development opportunities across PSI departments
- Flexible working hours
- Home-office option available, as well as combination of home and office work arrangement
- Extensive onboarding trainings and professional development training programs
- Highly developed company culture and positive team atmosphere
- Additional leave days (12 days of RTT)
- Please submit your CV/resume in English
Track this application
Keep your own notes. Only you can mark an application as sent.
Report a problem with this listing
Sign in to report this listing.
More at PSI CRO
Hybrid
Budapest, Budapest, Hungary
Full-time
Salary unavailable
Posted 2 months ago
Source: SmartRecruiters
Remote
Remote eligibility: Riga, Latvia
Full-time · Manager
Salary unavailable
Posted 2 months ago
Source: SmartRecruiters
Remote
Remote eligibility: Canada
Full-time
Salary unavailable
Posted 2 months ago
Source: SmartRecruiters
Hybrid
Munich, Bavaria, Germany
Full-time · Senior
Salary unavailable
Posted 2 months ago
Source: SmartRecruiters